autosomal recessive nonsyndromic deafness 35

Term ID

DOID:0110493

Synonyms

• autosomal recessive deafness 35
• DFNB35

Definition

An autosomal recessive nonsyndromic deafness that is characterized severe to profound hearing loss and has_material_basis_in mutation in the ESRRB gene on chromosome 14q24. https://www.ncbi.nlm.nih.gov/pubmed/18179891

References

• ICD10CM:H90.3
• OMIM:608565

Ontology

Human Disease   ( DOID:0110493 )